Evidence map›Paper›PMID 42195045›Full record

Observational studyGenes2026

Ralyath Balogoun, Margaux Serey-Gaut, Véronique Pingault, Isabelle Lemiere, Geneviève Lina-Granade, Geoffroy Delplancq, Anne Marie Guerrot, Annick Toutain, Delphine Dupin-Deguine, Marine Legendre and 4 more

Abstract readObservational Study
PubMed Full text at PMC Publisher
In one paragraph

Observational study in Genes, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Ralyath BalogounDepartment of Genomic Medicine for Rare Diseases, Necker-Enfants Malades Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), 75015 Paris, France.ORCID 0000-0002-1704-577X
Margaux Serey-GautDepartment of Genomic Medicine for Rare Diseases, Necker-Enfants Malades Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), 75015 Paris, France.ORCID 0000-0002-1165-0872
Véronique PingaultDepartment of Genomic Medicine for Rare Diseases, Necker-Enfants Malades Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), 75015 Paris, France.ORCID 0000-0001-7064-0765
Isabelle LemiereDepartment of Genomic Medicine for Rare Diseases, Necker-Enfants Malades Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), 75015 Paris, France.
Geneviève Lina-GranadeDepartment of Otorhinolaryngology and Audiophonology, Edouard Herriot Hospital, Hospices Civils de Lyon, 69437 Lyon, France.
Geoffroy DelplancqConstitutional Genetics Unit, Versailles Hospital, 78150 Versailles, France.
Anne Marie GuerrotInserm U1245, Department of Genetics and Reference Center for Developmental Disorders, Normandie University, University of Rouen Normandy, Rouen University Hospital (CHU Rouen), 76031 Rouen, France.
Annick ToutainDepartment of Medical Genetics, Tours University Hospital (CHRU Tours), 37044 Tours, France.ORCID 0000-0002-5999-5300
Delphine Dupin-DeguineDepartment of Otorhinolaryngology, Otoneurology and Pediatric Otorhinolaryngology, University of Toulouse, Purpan University Hospital (CHU Purpan), 31300 Toulouse, France.
Marine LegendreDepartment of Medical Genetics, Bordeaux University Hospital (CHU de Bordeaux), 33076 Bordeaux, France.
Estelle ColinInserm, CTM UMR1231, GAD Team, FHU TRANSLAD, Department of Genetics, Reference Center for Developmental Anomalies and Congenital Malformation Syndromes, Université Bourgogne, Dijon University Hospital (CHU Dijon Bourgogne), 21079 Dijon, France.
Natalie LoundonDepartment of Pediatric Otorhinolaryngology and Head and Neck Surgery, Necker-Enfants Malades Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris Cité University, 75015 Paris, France.
Laurence JonardDepartment of Genomic Medicine for Rare Diseases, Necker-Enfants Malades Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), 75015 Paris, France.ORCID 0000-0003-0369-0505
Sandrine MarlinDepartment of Genomic Medicine for Rare Diseases, Necker-Enfants Malades Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), 75015 Paris, France.ORCID 0000-0002-4115-9806

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Extracellular Matrix ProteinsHearing Loss, SensorineuralAdolescentAdultChildChild, PreschoolFemaleFranceGenetic Association StudiesHumansMaleMiddle AgedMutationPedigreePhenotypeRetrospective StudiesCOCH protein, humanExtracellular Matrix Proteinsautosomal dominant NSHLCOCHDFNA9genotype–phenotypehearing lossnovel variantvestibular dysfunction

Identifiers

PMID42195045
PMCPMC13206081

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.